Age, Gene/Environment Susceptibility-Reykjavik Study: Multidisciplinary applied phenomics

被引:452
作者
Harris, Tamara B.
Launer, Lenore J.
Eiriksdottir, Gudny
Kjartansson, Olafur
Jonsson, Palmi V.
Sigurdsson, Gunnar
Thorgeirsson, Gudmundur
Aspelund, Thor
Garcia, Melissa E.
Cotch, Mary Frances
Hoffman, Howard J.
Gudnason, Vilmundur
机构
[1] NIA, Lab Epidemiol Demog & Biometry, Intramural Res Program, Bethesda, MD 20892 USA
[2] Icelandic Heart Assoc, Kopavogur, Iceland
[3] Landspitali Univ Hosp, Dept Radiol, Reykjavik, Iceland
[4] Landspitali Univ Hosp, Dept Geriatr, Reykjavik, Iceland
[5] Univ Iceland, Fac Med, Reykjavik, Iceland
[6] Landspitali Univ Hosp, Dept Endocrinol & Metab, Reykjavik, Iceland
[7] Landspitali Univ Hosp, Dept Med, Reykjavik, Iceland
[8] NEI, Div Epidemiol & Clin Res, Bethesda, MD 20892 USA
[9] NIDCD, Epidemiol & Biostat Program, Bethesda, MD USA
关键词
aging; body composition; cardiovascular diseases; cognition; genetics; population; osteoporosis; phenotype;
D O I
10.1093/aje/kwk115
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
In anticipation of the sequencing of the human genome and description of the human proteome, the Age, Gene/ Environment Susceptibility-Reykjavik Study (AGES-Reykjavik) was initiated in 2002. AGES-Reykjavik was designed to examine risk factors, including genetic susceptibility and gene/environment interaction, in relation to disease and disability in old age. The study is multidisciplinary, providing detailed phenotypes related to the cardiovascular, neurocognitive (including sensory), and musculoskeletal systems, and to body composition and metabolic regulation. Relevant quantitative traits, subdinical indicators of disease, and medical diagnoses are identified by using biomarkers, imaging, and other physiologic indicators. The AGES-Reykjavik sample is drawn from an established population-based cohort, the Reykjavik Study. This cohort of men and women born between 1907 and 1935 has been followed in Iceland since 1967 by the Icelandic Heart Association. The AGES-Reykjavik cohort, with cardiovascular risk factor assessments earlier in life and detailed late-life phenotypes of quantitative traits, will create a comprehensive study of aging nested in a relatively genetically homogeneous older population. This approach should facilitate identification of genetic factors that contribute to healthy aging as well as the chronic conditions common in old age.
引用
收藏
页码:1076 / 1087
页数:12
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